NDC product
EXTRA FAST COLTALIN
NDC 51467-014 · FORTUNE PHARMACAL COMPANY LIMITED
Key facts
| Product NDC | 51467-014 |
|---|---|
| Proprietary name | EXTRA FAST COLTALIN |
| Nonproprietary name | Acetaminophen, Chlorpheniramine maleate, Phenylephrine hydrochloride |
| Substances | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HYDROCHLORIDE |
| Dosage form | TABLET |
| Route | ORAL |
| Labeler | FORTUNE PHARMACAL COMPANY LIMITED |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M012 |
| Pharmacologic classes | Adrenergic alpha1-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-1 Adrenergic Agonist [EPC] |
| Marketing start | Jul 1, 2025 |
| Marketing end | Jun 30, 2029 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory